Fosfomycin Resistance Evolutionary Pathways of Stenotrophomonas maltophilia in Different Growing Conditions

Int J Mol Sci. 2022 Jan 20;23(3):1132. doi: 10.3390/ijms23031132.

Abstract

The rise of multidrug-resistant Gram-negative pathogens and the lack of novel antibiotics to address this problem has led to the rescue of old antibiotics without a relevant use, such as fosfomycin. Stenotrophomonas maltophilia is a Gram-negative, non-fermenter opportunistic pathogen that presents a characteristic low susceptibility to several antibiotics of common use. Previous work has shown that while the so-far described mechanisms of fosfomycin resistance in most bacteria consist of the inactivation of the target or the transporters of this antibiotic, as well as the production of antibiotic-inactivating enzymes, these mechanisms are not selected in S. maltophilia fosfomycin-resistant mutants. In this microorganism, fosfomycin resistance is caused by the inactivation of enzymes belonging to its central carbon metabolism, hence linking metabolism with antibiotic resistance. Consequently, it is relevant to determine how different growing conditions, including urine and synthetic sputum medium that resemble infection, could impact the evolutionary pathways towards fosfomycin resistance in S. maltophilia. Our results show that S. maltophilia is able to acquire high-level fosfomycin resistance under all tested conditions. However, although some of the genetic changes leading to resistance are common, there are specific mutations that are selected under each of the tested conditions. These results indicate that the pathways of S. maltophilia evolution can vary depending on the infection point and provide information for understanding in more detail the routes of fosfomycin resistance evolution in S. maltophilia.

Keywords: Stenotrophomonas maltophilia; experimental evolution; fosfomycin resistance.

MeSH terms

  • Adult
  • Bacterial Proteins / genetics*
  • Bacteriological Techniques
  • Carbon / metabolism
  • Drug Resistance, Multiple, Bacterial*
  • Evolution, Molecular
  • Female
  • Fosfomycin / pharmacology*
  • Gene Expression Regulation, Bacterial / drug effects
  • Humans
  • Male
  • Microbial Sensitivity Tests
  • Middle Aged
  • Mutation
  • Stenotrophomonas maltophilia / drug effects
  • Stenotrophomonas maltophilia / genetics
  • Stenotrophomonas maltophilia / growth & development*

Substances

  • Bacterial Proteins
  • Fosfomycin
  • Carbon